Suppr超能文献

瘦素、骨骼肌脂质与脂质诱导的胰岛素抵抗。

Leptin, skeletal muscle lipids, and lipid-induced insulin resistance.

作者信息

Dube John J, Bhatt Bankim A, Dedousis Nikolas, Bonen Arend, O'Doherty Robert M

机构信息

Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2007 Aug;293(2):R642-50. doi: 10.1152/ajpregu.00133.2007. Epub 2007 May 9.

Abstract

Leptin-induced increases in insulin sensitivity are well established and may be related to the effects of leptin on lipid metabolism. However, the effects of leptin on the levels of lipid metabolites implicated in pathogenesis of insulin resistance and the effects of leptin on lipid-induced insulin resistance are unknown. The current study addressed in rats the effects of hyperleptinemia (HL) on insulin action and markers of skeletal muscle (SkM) lipid metabolism in the absence or presence of acute hyperlipidemia induced by an infusion of a lipid emulsion. Compared with controls (CONT), HL increased insulin sensitivity, as assessed by hyperinsulinemic-euglycemic clamp ( approximately 15%), and increased SkM Akt ( approximately 30%) and glycogen synthase kinase 3 alpha ( approximately 52%) phosphorylation. These improvements in insulin action were associated with decreased SkM triglycerides (TG; approximately 61%), elevated ceramides ( approximately 50%), and similar diacylglycerol (DAG) levels in HL compared with CONT. Acute hyperlipidemia in CONT decreased insulin sensitivity ( approximately 25%) and increased SkM DAG ( approximately 33%) and ceramide ( approximately 60%) levels. However, hyperlipidemia did not induce insulin resistance or SkM DAG and ceramide accumulation in HL. SkM total fatty acid transporter CD36, plasma membrane fatty acid binding protein, acetyl Co-A carboxylase phosphorylation, and fatty acid oxidation were similar in HL compared with CONT. However, HL decreased SkM protein kinase C theta (PKC theta), a kinase implicated in mediating the detrimental effects of lipids on insulin action. We conclude that increases in insulin sensitivity induced by HL are associated with decreased levels of SkM TG and PKC theta and increased SkM insulin signaling, but not with decreases in other lipid metabolites implicated in altering SkM insulin sensitivity (DAG and ceramide). Furthermore, insulin resistance induced by an acute lipid infusion is prevented by HL.

摘要

瘦素诱导的胰岛素敏感性增加已得到充分证实,可能与瘦素对脂质代谢的影响有关。然而,瘦素对参与胰岛素抵抗发病机制的脂质代谢产物水平的影响以及瘦素对脂质诱导的胰岛素抵抗的影响尚不清楚。本研究探讨了在大鼠中,高脂血症(HL)在输注脂质乳剂诱导的急性高脂血症存在或不存在的情况下,对胰岛素作用和骨骼肌(SkM)脂质代谢标志物的影响。与对照组(CONT)相比,通过高胰岛素-正常血糖钳夹评估,HL增加了胰岛素敏感性(约15%),并增加了SkM Akt(约30%)和糖原合酶激酶3α(约52%)的磷酸化。与CONT相比,HL中胰岛素作用的这些改善与SkM甘油三酯(TG;约61%)降低、神经酰胺升高(约50%)以及二酰甘油(DAG)水平相似有关。CONT中的急性高脂血症降低了胰岛素敏感性(约25%),并增加了SkM DAG(约33%)和神经酰胺(约60%)水平。然而,高脂血症并未在HL中诱导胰岛素抵抗或SkM DAG和神经酰胺积累。与CONT相比,HL中SkM总脂肪酸转运蛋白CD36、质膜脂肪酸结合蛋白、乙酰辅酶A羧化酶磷酸化和脂肪酸氧化相似。然而,HL降低了SkM蛋白激酶Cθ(PKCθ),这是一种与介导脂质对胰岛素作用的有害影响有关的激酶。我们得出结论,HL诱导的胰岛素敏感性增加与SkM TG和PKCθ水平降低以及SkM胰岛素信号增加有关,但与其他参与改变SkM胰岛素敏感性的脂质代谢产物(DAG和神经酰胺)的降低无关。此外,HL可预防急性脂质输注诱导的胰岛素抵抗。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验